HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279068Generated: November 1, 2026
3-Bromo-6-chloroimidazo(1,2-b)pyridazine → 6-Chloro-3-(3-methoxypyridazin-4-yl)imidazo[1,2-b]pyridazine
https://huagongshe.com/reaction/2279068
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromo-6-chloroimidazo(1,2-b)pyridazine | HCID 12872323 | — |
| Reactant | 3-Methoxy-4-(tributylstannyl)pyridazine | HCID 67485729 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-3-(3-methoxypyridazin-4-yl)imidazo[1,2-b]pyridazine | HCID 86702327 | 64.2% |
Reaction Steps
A mixture of 3-bromo-6-chloroimidazo[1,2-b]pyridazine (Preparation 1b, 182 mg, 0.78 mmol), 3-methoxy-4-(tributylstannyl)pyridazine (Preparation 8b, 313 mg, 0.78 mmol), copper(I) iodide (15 mg, 0.08 mmol) and dry N,N′-dimethylformamide (4 mL) in a Schlenk vial was subjected to three cycles of evacuation backfilling with argon. Tetrakis(triphenylphosphine)palladium(0) (91 mg, 0.08 mmol) was then added and the resulting mixture was subjected to three further cycles of evacuation backfilling with argon before being stirred at 100° C. for 20 hours. The reaction mixture was cooled down, the solvent was removed under reduced pressure and the residue was purified by flash chromatography (1:1 hexanes/ethyl acetate to 100% ethyl acetate) to give the title compound (131 mg, 64%) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133200B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-6d5d64b71fbf48d6a37a2caf250cbbf9 |
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| Source note | uspto-grants-2015_09 |
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